生物
Cre重组酶
转基因
造血
Cre-Lox重组
分子生物学
转基因小鼠
重组酶
基因靶向
细胞培养
细胞生物学
位点特异性重组
基因
干细胞
遗传学
重组
作者
Jasper de Boer,Adam Williams,George Skavdis,Nicola Harker,Mark Coles,Mauro Tolaini,Trisha Norton,Keith L. Williams,Kathleen Roderick,Alexandre J. Potocnik,Dimitris Kioussis
标识
DOI:10.1002/immu.200310005
摘要
Abstract Bacteriophage P1 Cre/loxP based systems can be used to manipulate the genomes of mice in vivo and in vitro, allowing the generation of tissue‐specific conditional mutants. Wehave generated mouse lines expressing Cre recombinase in hematopoietic tissues using the vav regulatory elements, or in lymphoid cells using the hCD2 promoter and locus control region (LCR). The R26R‐EYFP Cre reporter mouse line was used to determine the pattern of Cre expression in each line and enabled the assessment of Cre activity at a single‐cell level. Analysis showed that the vav promoter elements were able to direct Cre‐mediated recombination in all cells of the hematopoietic system. The hCD2 promoter and LCR on the other hand were able to drive Cre‐mediated recombination only in T cells and B cells, but not in other hematopoietic cell types. Furthermore, in the appropriate tissues, deletion of the floxed target was complete in all cells, thereby excluding the possibility of variegated expression of the Cre transgene. Both of these Cre‐transgenic lines will be useful in generating tissue‐specific gene deletions within all the cells of hematopoietic or lymphoid tissues.
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